| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:45584765-45585054 | Common:4; Rare:111; Clinvar:2; Clinvar (benign):4 | ||||
| chr19:45642402-45642681 | Common:1; Rare:65 | ||||
| chr19:45692361-45692722 | Common:1; Rare:86 | ||||
| chr19:45730869-45731092 | Common:1; Rare:52 | ||||
| chr19:45863116-45863359 | Common:3; Rare:80 | ||||
| chr19:46346939-46347156 | Common:3; Rare:76 | ||||
| chr19:46600913-46601406 | Common:5; Rare:168 | ||||
| chr19:46608292-46608487 | Common:1; Rare:53; Clinvar (benign):4 | ||||
| chr19:46745835-46746061 | Common:3; Rare:46 | ||||
| chr19:46784750-46785064 | Common:1; Rare:70 | ||||
| chr19:46787270-46787525 | Common:1; Rare:72 | ||||
| chr19:46787687-46787980 | Common:1; Rare:82 | ||||
| chr19:46788430-46788629 | Rare:47 | ||||
| chr19:46850238-46850381 | Rare:19 | ||||
| chr19:47112151-47112493 | Rare:109 |